FDA NDC Directory · JSON-LD · Markdown
NDC 72887-683 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | oxycodone and acetaminophen tablets |
|---|---|
| Labeler / Manufacturer | FH2 Pharma LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA040608 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | ACETAMINOPHEN (300 mg/1) OXYCODONE HYDROCHLORIDE (10 mg/1) |
| Marketing started | 20200701 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).